http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2290194-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_23a4e0c875bf1ac2b8a3b76517de6c7d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C309-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-255
filingDate 1974-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db13297d48e4a15705f457e50d8ecfc6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_83bcb08b4781b4856eb6afab4a6ec071
publicationDate 1976-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2290194-A1
titleOfInvention SULPHONATES (ESTERS) USED AS CHOLESTEROL DECREASING AGENTS
abstract Sulphonic acid esters have the formula (I): R-SO3 -mR' (I) (where R is cyclo-hexadienyl, cyclohexadienyl opt. substd. by 1-12C alkyl, phenylcyclohexadienyl, naphthyl substd. by 1-12C alkyl, indanyl, cyclohexenyl opt. substd. by 1-12C alkyl, phenylcyclohexenyl, cycloheyl substd. by 1-12c alkyl, phenylcyclohexyl, n is 1, 2 or 3 and when n is 1 Y is 2-20C alkyl, phenyl halogen, 1-3 C alkoxy 2-3C alkenyl, CO, NO2, halomethyl or phenylazo and when n is 2 or 3 each group is independently 1-20C alkyl, phenyl, halogen, 1-3C alkoxy, 2-3C alkenyl, carboxyl, NO2, halomethyl or phenyl azo; X is H Ph, PhCH2, 1-12C alkyl, 1-12C alkylbenzyl or 1-12C alkylphenyl; m is 1 or 2 and R' is an opt. unsatd. 8-25C group contg. at least 8C in a straight chain and linked to SO3 through a primary or secondary C atom). (I) are used for reducing the blood cholesterol level.
priorityDate 1974-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 29.